FDAFDA · Food and drugs·Recall number Z-2261-2024
This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225
Published July 10, 2024 · Recall initiated: June 3, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Expired Products distributed to customers
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Corporation
- Distributor
- US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
- Lot
- GTIN: 07613327118438 Lot Number: 1000388946
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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